A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003893



Internal ID18746424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107993422..108023690hg38UCSC Ensembl
Innerchr4:108914578..108944846hg19UCSC Ensembl
Innerchr4:109134027..109164295hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3830269
hg1930269
hg1830269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632597
Samples
Known GenesHADH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003893
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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